EP2298778A4 - Dérivé d imidazothiazole ayant une structure cyclique de 4,7-diazaspiroý2.5¨octane - Google Patents

Dérivé d imidazothiazole ayant une structure cyclique de 4,7-diazaspiroý2.5¨octane

Info

Publication number
EP2298778A4
EP2298778A4 EP09762499A EP09762499A EP2298778A4 EP 2298778 A4 EP2298778 A4 EP 2298778A4 EP 09762499 A EP09762499 A EP 09762499A EP 09762499 A EP09762499 A EP 09762499A EP 2298778 A4 EP2298778 A4 EP 2298778A4
Authority
EP
European Patent Office
Prior art keywords
imidazothiazole
diazaspiro
derivate
cyclic structure
cyclic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP09762499A
Other languages
German (de)
English (en)
Other versions
EP2298778A1 (fr
Inventor
Kouichi Uoto
Haruko Kawato
Yuuichi Sugimoto
Hiroyuki Naito
Masaki Miyazaki
Toru Taniguchi
Masashi Aonuma
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Daiichi Sankyo Co Ltd
Original Assignee
Daiichi Sankyo Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daiichi Sankyo Co Ltd filed Critical Daiichi Sankyo Co Ltd
Publication of EP2298778A1 publication Critical patent/EP2298778A1/fr
Publication of EP2298778A4 publication Critical patent/EP2298778A4/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
EP09762499A 2008-06-12 2009-06-10 Dérivé d imidazothiazole ayant une structure cyclique de 4,7-diazaspiroý2.5¨octane Withdrawn EP2298778A4 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2008154036 2008-06-12
PCT/JP2009/060575 WO2009151069A1 (fr) 2008-06-12 2009-06-10 Dérivé d’imidazothiazole ayant une structure cyclique de 4,7-diazaspiro[2.5]octane

Publications (2)

Publication Number Publication Date
EP2298778A1 EP2298778A1 (fr) 2011-03-23
EP2298778A4 true EP2298778A4 (fr) 2011-10-05

Family

ID=41416775

Family Applications (1)

Application Number Title Priority Date Filing Date
EP09762499A Withdrawn EP2298778A4 (fr) 2008-06-12 2009-06-10 Dérivé d imidazothiazole ayant une structure cyclique de 4,7-diazaspiroý2.5¨octane

Country Status (4)

Country Link
EP (1) EP2298778A4 (fr)
JP (1) JPWO2009151069A1 (fr)
TW (1) TW201002724A (fr)
WO (1) WO2009151069A1 (fr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT2380892E (pt) * 2009-01-16 2014-06-09 Daiichi Sankyo Co Ltd Derivado de imidazotiazole compreendendo uma estrutura de anel prolina
KR20120099462A (ko) 2009-11-12 2012-09-10 더 리젠츠 오브 더 유니버시티 오브 미시건 스피로-옥신돌 mdm2 길항제
AU2011326395B2 (en) 2010-11-12 2016-01-07 Ascenta Licensing Corporation Spiro-oxindole MDM2 antagonists
US8629141B2 (en) 2011-05-11 2014-01-14 The Regents Of The University Of Michigan Spiro-oxindole MDM2 antagonists
TW201429969A (zh) 2012-12-20 2014-08-01 Merck Sharp & Dohme 作爲hdm2抑制劑之經取代咪唑吡啶
US20170216286A1 (en) 2014-01-28 2017-08-03 Mayo Foundation For Medical Education And Research Killing senescent cells and treating senescence-associated conditions using a src inhibitor and a flavonoid
US10328058B2 (en) 2014-01-28 2019-06-25 Mayo Foundation For Medical Education And Research Treating atherosclerosis by removing senescent foam cell macrophages from atherosclerotic plaques
AU2015211021B2 (en) 2014-01-28 2020-07-02 Buck Institute For Research On Aging Methods and compositions for killing senescent cells and for treating senescence-associated diseases and disorders
CN105111155B (zh) * 2015-08-31 2018-12-14 武汉工程大学 一种4,7-二氮杂螺[2.5]辛烷-7-甲酸叔丁酯的合成方法
WO2017176958A1 (fr) 2016-04-06 2017-10-12 The Regents Of The University Of Michigan Intermédiaires monofonctionnels pour la dégradation d'une protéine cible dépendante du ligand
AU2017246452C1 (en) 2016-04-06 2021-06-03 The Regents Of The University Of Michigan MDM2 protein degraders
EP3458101B1 (fr) 2016-05-20 2020-12-30 H. Hoffnabb-La Roche Ag Conjugués anticorps-protac et procédés d'utilisation
CN108530375B (zh) * 2018-05-29 2020-04-21 南京药石科技股份有限公司 4-氧杂-7-氮杂螺[2.5]辛烷或其盐的中间体及制备方法
CN111943894A (zh) * 2019-05-17 2020-11-17 南京爱德程医药科技有限公司 一种4,7-二氮杂螺[2.5]辛烷类化合物的合成方法
CN111943893B (zh) * 2019-05-17 2024-07-26 南京爱德程医药科技有限公司 4,7-二氮杂螺[2,5]辛烷类化合物的合成方法
WO2023056069A1 (fr) 2021-09-30 2023-04-06 Angiex, Inc. Conjugués agent de dégradation-anticorps et leurs procédés d'utilisation
WO2023165523A1 (fr) * 2022-03-01 2023-09-07 上海璎黎药业有限公司 Dérivé méthoxy substitué par un cycle aromatique et son utilisation
WO2024240858A1 (fr) 2023-05-23 2024-11-28 Valerio Therapeutics Molécules protac dirigées contre un système de réparation de dommages à l'adn et leurs utilisations

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1167369A1 (fr) * 1999-04-06 2002-01-02 Yamanouchi Pharmaceutical Co. Ltd. Nouveaux derives de thiazolobenzimidazole
US6696441B1 (en) * 2000-08-11 2004-02-24 The Regents Of The University Of California Inhibition of p53-induced stress response
EP1486501A1 (fr) * 2002-03-20 2004-12-15 Yamanouchi Pharmaceutical Co. Ltd. Derive de thiazolobenzimidazole substitue par aminomethyle
WO2010082612A1 (fr) * 2009-01-16 2010-07-22 第一三共株式会社 Dérivé d'imidazothiazole comprenant une structure de noyau proline

Family Cites Families (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US526916A (en) 1894-10-02 Milking-stool
WO1997048706A1 (fr) 1996-06-18 1997-12-24 Warner-Lambert Company Pyrrolo(1,2-a)pyrazine 1,4-diones servant d'inhibiteurs des serines proteases
US6238921B1 (en) 1998-03-26 2001-05-29 Isis Pharmaceuticals, Inc. Antisense oligonucleotide modulation of human mdm2 expression
JP2000072743A (ja) 1998-08-31 2000-03-07 Japan Science & Technology Corp アルケンのアジリジン化法
GB9819860D0 (en) 1998-09-12 1998-11-04 Zeneca Ltd Chemical compounds
US6979551B2 (en) 2000-04-03 2005-12-27 Rigel Pharmaceuticals, Inc. Assays for identifying ubiquitin agents and for identifying agents that modify the activity of ubiquitin agents
US6740495B1 (en) 2000-04-03 2004-05-25 Rigel Pharmaceuticals, Inc. Ubiquitin ligase assay
PT1443937E (pt) 2001-11-13 2008-09-23 Ortho Mcneil Janssen Pharm 1,4-benzodiazepinas substituídas e as suas utilizações para o tratamento de cancro
BR0215156A (pt) 2001-12-18 2004-10-19 Hoffmann La Roche Cis-imidazolinas como inibidores de mdm 2
BR0215157A (pt) 2001-12-18 2004-10-19 Hoffmann La Roche Cis-2,4,5-trifenil-imidazolinas e seu uso no tratamento de tumores
WO2003095625A2 (fr) 2002-05-13 2003-11-20 3-Dimensional Pharmaceuticals, Inc. Procede de cytoprotection par inhibition de mdm2 et de hdm2
GB0215650D0 (en) * 2002-07-05 2002-08-14 Cyclacel Ltd Bisarylsufonamide compounds
US20040197893A1 (en) 2002-10-16 2004-10-07 Carsten Schubert HDM2-inhibitor complexes and uses thereof
GB0225548D0 (en) 2002-11-01 2002-12-11 Glaxo Group Ltd Compounds
US6916833B2 (en) 2003-03-13 2005-07-12 Hoffmann-La Roche Inc. Substituted piperidines
WO2004094407A1 (fr) 2003-04-21 2004-11-04 Daiichi Pharmaceutical Co. Ltd. Derive heterocyclique a cinq chainons
US20040213264A1 (en) 2003-04-25 2004-10-28 Nortel Networks Limited Service class and destination dominance traffic management
UA82230C2 (en) 2003-04-25 2008-03-25 Орто-Макнейл Фармасьютикел, Инк. Substituted 1,4-diazepines and uses thereof
GB0309637D0 (en) * 2003-04-28 2003-06-04 Cancer Rec Tech Ltd Pyrazole compounds
US7425638B2 (en) 2003-06-17 2008-09-16 Hoffmann-La Roche Inc. Cis-imidazolines
CN100562316C (zh) 2003-06-17 2009-11-25 霍夫曼-拉罗奇有限公司 作为mdm2抑制剂的顺式咪唑啉
AU2004254187A1 (en) 2003-06-17 2005-01-13 F. Hoffmann-La Roche Ag Cis-2,4,5-triaryl-imidazolines
US7132421B2 (en) 2003-06-17 2006-11-07 Hoffmann-La Roche Inc. CIS-imidazoles
GB0324498D0 (en) 2003-07-21 2003-11-26 Aventis Pharma Inc Heterocyclic compounds as P2X7 ion channel blockers
JP2005075754A (ja) 2003-08-29 2005-03-24 Mitsui Chemicals Inc トランス−1,2−ビス(3,5−ジメチルフェニル)−1,2−エタンジアミンの光学分割方法
JP2005306839A (ja) * 2003-08-29 2005-11-04 Takeda Chem Ind Ltd 二環性ピペラジン化合物およびその用途
BRPI0511328A (pt) 2004-05-18 2007-12-04 Hoffmann La Roche cis-imidazolinas
US7893278B2 (en) 2004-06-17 2011-02-22 Hoffman-La Roche Inc. CIS-imidazolines
GB0419481D0 (en) 2004-09-02 2004-10-06 Cancer Rec Tech Ltd Isoindolin-1-one derivatives
KR100944301B1 (ko) 2005-02-22 2010-02-24 더 리젠츠 오브 더 유니버시티 오브 미시간 Mdm2의 소분자 억제제 및 이의 용도
JP4955646B2 (ja) 2005-03-16 2012-06-20 エフ.ホフマン−ラ ロシュ アーゲー シス−2,4,5−トリアリール−イミダゾリン及びそれらの抗癌薬としての使用
US8211919B2 (en) 2005-09-02 2012-07-03 Astellas Pharma Inc. Amide derivatives as rock inhibitors
CN101316823B (zh) 2005-12-01 2013-05-22 霍夫曼-拉罗奇有限公司 用作抗癌剂的作为p53和MDM2蛋白之间相互作用的抑制剂的2,4,5-三苯基咪唑啉衍生物
SG174107A1 (en) 2006-08-30 2011-09-29 Univ Michigan New small molecule inhibitors of mdm2 and the uses thereof
AU2007332493A1 (en) * 2006-12-14 2008-06-19 Daiichi Sankyo Company, Limited Imidazothiazole derivatives
PL2134720T3 (pl) 2007-03-29 2011-04-29 Novartis Ag Heterocykliczne spiro-związki

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1167369A1 (fr) * 1999-04-06 2002-01-02 Yamanouchi Pharmaceutical Co. Ltd. Nouveaux derives de thiazolobenzimidazole
US6696441B1 (en) * 2000-08-11 2004-02-24 The Regents Of The University Of California Inhibition of p53-induced stress response
EP1486501A1 (fr) * 2002-03-20 2004-12-15 Yamanouchi Pharmaceutical Co. Ltd. Derive de thiazolobenzimidazole substitue par aminomethyle
WO2010082612A1 (fr) * 2009-01-16 2010-07-22 第一三共株式会社 Dérivé d'imidazothiazole comprenant une structure de noyau proline

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2009151069A1 *

Also Published As

Publication number Publication date
TW201002724A (en) 2010-01-16
EP2298778A1 (fr) 2011-03-23
JPWO2009151069A1 (ja) 2011-11-17
WO2009151069A1 (fr) 2009-12-17

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